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Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists.
J Med Chem. 2005 Dec 1;48(24):7882-905. doi: 10.1021/jm050645f.
J Med Chem. 2005.
PMID: 16302826
Discovery of a new class of potent, selective, and orally bioavailable CRTH2 (DP2) receptor antagonists for the treatment of allergic inflammatory diseases.
Crosignani S, Page P, Missotten M, Colovray V, Cleva C, Arrighi JF, Atherall J, Macritchie J, Martin T, Humbert Y, Gaudet M, Pupowicz D, Maio M, Pittet PA, Golzio L, Giachetti C, Rocha C, Bernardinelli G, Filinchuk Y, Scheer A, Schwarz MK, Chollet A.
Crosignani S, et al. Among authors: colovray v.
J Med Chem. 2008 Apr 10;51(7):2227-43. doi: 10.1021/jm701383e. Epub 2008 Mar 5.
J Med Chem. 2008.
PMID: 18318469
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Optimization of the Central Core of Indolinone-Acetic Acid-Based CRTH2 (DP2) Receptor Antagonists.
Crosignani S, Jorand-Lebrun C, Page P, Campbell G, Colovray V, Missotten M, Humbert Y, Cleva C, Arrighi JF, Gaudet M, Johnson Z, Ferro P, Chollet A.
Crosignani S, et al. Among authors: colovray v.
ACS Med Chem Lett. 2011 Jun 9;2(8):644-9. doi: 10.1021/ml2001196. eCollection 2011 Aug 11.
ACS Med Chem Lett. 2011.
PMID: 24900359
Free PMC article.
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Design and synthesis of new potent, silent 5-HT1A antagonists by covalent coupling of aminopropanol derivatives with selective serotonin reuptake inhibitors.
Perez M, Pauwels PJ, Pallard-Sigogneau I, Fourrier C, Chopin P, Palmier C, Colovray V, Halazy S.
Perez M, et al. Among authors: colovray v.
Bioorg Med Chem Lett. 1998 Dec 1;8(23):3423-8. doi: 10.1016/s0960-894x(98)00619-2.
Bioorg Med Chem Lett. 1998.
PMID: 9873746
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